Hybrid coatings and associated methods of application

ABSTRACT

A hybrid coating composition including an organosilane component, a metal alkoxide component and a surfactant component, with the metal alkoxide component present in the composition at a molar ratio of about 75:1 with respect to the surfactant component. The hybrid coating composition once cured on a transparent substrate has an initial clarity greater than 98. Transparent members are also disclosed that include a transparent substrate having the hybrid coating composition cured on a first major surface thereof.

RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No.12/363,085, filed Jan. 30, 2009.

FIELD

The present patent application relates to hybrid abrasion resistantcoatings, methods for making the hybrid abrasion coatings, andassociated methods for treating and replenishing surfaces subject towear.

BACKGROUND

The effects of wear on mechanical parts and exposed surfaces areprevalent in various applications. The effects of wear are particularlyprevalent in connection with transparent parts and surfaces that requireclarity. For example, the windows of aircraft are subjected to wear bothin flight and on the ground.

Accordingly, scientists and engineers continue to search for coatingsthat resist the effects of wear, thereby reducing the time and expenseassociated with maintenance by extending the time intervals betweensuccessive replacement/repair operations. Furthermore, scientists andengineers continue to search for coatings that may be used to restorescratched and worn substrates, thereby reducing maintenance costs byfacilitating the repair of substrates that would otherwise requirereplacement. Environmentally friendly coatings would be particularlyattractive.

SUMMARY

In one aspect, the disclosed hybrid coating may include a mixture of anorganosilane component, a metal alkoxide component and a surfactantcomponent, with the metal alkoxide component present in the compositionat a molar ratio of about 75:1 with respect to the surfactant component.This hybrid coating composition once cured on a transparent substratehas an initial clarity greater than 98.

The hybrid coating composition may also include water and be a sol gel.In one embodiment, the hybrid coating composition is substantially freeof particles greater than 11 μm.

The organosilane may be one or more of(3-glycidoxypropyl)trimethoxysilane, 3-glycidoxypropyltriethoxysilane,paminophenylsilane, allyltrimethoxysilane,n-(2-aminoethyl)-3-aminopropyltrimethoxysilane,3-aminopropyltriethoxysilane, 3-aminopropyltrimethoxysilane,3-glycidoxypropyldiisopropylethoxysilane,(3-glycidoxypropyl)methyldiethoxysilane,3-mercaptopropyltrimethoxysilane, 3-mercaptopropyltriethoxysilane,3-methacryloxypropylmethyldiethoxysilane,3-methacryloxypropylmethyldimethoxysilane,3methacryloxypropyltrimethoxysilane,n-phenylaminopropyltrimethoxysilane, vinylmethyldiethoxysilane,vinyltriethoxysilane, vinyltrimethoxysilane, tetraethylorthosilicate.

The metal alkoxide may be one or more of aluminum s-butoxide, aluminumn-butoxide, and aluminum t-butoxide or one or more of cerium IVisopropoxide, cerium IV methoxyethoxide, and cerium III2,4-pentanedionate. The surfactant component may be a straight chainprimary aliphatic alkoxylated alcohol.

In another aspect, the disclosed hybrid coating may include a mixture of(3-glycidoxypropyl)trimethoxysilane, aluminum s-butoxide and asurfactant component, wherein the mixture is substantially free ofparticles greater than about 11 μm.

In another aspect, transparent members are disclosed that include atransparent substrate having the hybrid coating composition disclosedherein cured on a first major surface thereof. The first major surfaceof the transparent substrate may be an oxygen plasma treated surface ora corona treated surface with the hybrid coating composition curedthereto.

In one embodiment, the transparent member may also include an adhesionpromoter between the transparent substrate and the hybrid coatingcomposition. The adhesion promoter may include a solution of3-aminopropyltriethoxysilane in water.

In one embodiment, the transparent substrate is a window or windshieldcomprising stretched acrylic or glass.

Other aspects of the disclosed hybrid coatings and associated methods ofapplication will become apparent from the following description, theaccompanying drawings and the appended claims.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a flow chart illustrating one exemplary method for applyingthe disclosed hybrid coating;

FIG. 2 is a graphical illustration of percent haze obtained after 100cycles of Taber abrasion on an untreated substrate (“Bare Acrylic”), asubstrate treated with a prior art coating (“Polysiloxane”), and asubstrate treated with an aspect of the disclosed hybrid coating(“Hybrid”);

FIG. 3 is a graphical illustration of percent haze versus number ofTaber abrasion cycles for a bare acrylic substrate and an acrylicsubstrate coated with the disclosed hybrid coating;

FIG. 4 is a graphical illustration of percent haze versus number ofTaber abrasion cycles for an worn acrylic substrate replenished with thedisclosed hybrid coating;

FIG. 5 is a graphical illustration of percent haze versus number ofTaber abrasion cycles for an acrylic substrate coated with the disclosedhybrid coating, subjected to abrasion, replenished with the disclosedhybrid coating, then again subjected to abrasion;

FIG. 6 is a graphical illustration of percent haze versus number ofTaber abrasion cycles for an acrylic substrate coated with a prior artcoating, subjected to abrasion, replenished with the disclosed hybridcoating, then again subjected to abrasion;

FIG. 7 is a graphical illustration of percent haze versus number ofTaber abrasion cycles for an acrylic substrate initially coated with aduplex coating (i.e., a first layer of prior art coating with a top coatof the disclosed hybrid coating), subjected to abrasion, replenishedwith the disclosed hybrid coating, then again subjected to abrasion; and

FIG. 8 is a flow chart illustrating one exemplary method for making thedisclosed hybrid coating.

DETAILED DESCRIPTION

In one aspect, the disclosed hybrid coating may include an organosilanecomponent, a metal alkoxide component and a surfactant component. Watermay be added to, for example, adjust the solids content and/or viscosityof the mixture. Additional components having various functionalities,such as, for example, dyes, light scavengers, rheology modifiers andbiocides, may be added to the disclosed hybrid coating without departingfrom the scope of the present disclosure.

The organosilane component may be the organic portion of the disclosedhybrid coating. In one exemplary aspect, the organosilane component maybe (3-glycidoxypropyl)trimethoxysilane. However, alternative examples ofcompounds useful as the organosilane component include3-glycidoxypropyltriethoxysilane, p-aminophenylsilane,allyltrimethoxysilane, n-(2-aminoethyl)-3-aminopropyltrimethoxysilane,3-aminopropyltriethoxysilane, 3-aminopropyltrimethoxysilane,3-glycidoxypropyldiisopropylethoxysilane,(3-glycidoxypropyl)methyldiethoxysilane,3-mercaptopropyltrimethoxysilane, 3-mercaptopropyltriethoxysilane,3-methacryloxypropylmethyldiethoxysilane,3-methacryloxypropylmethyldimethoxysilane,3-methacryloxypropyltrimethoxysilane,n-phenylaminopropyltrimethoxysilane, vinylmethyldiethoxysilane,vinyltriethoxysilane, vinyltrimethoxysilane and tetraethylorthosilicate,as well as combinations thereof. Those skilled in the art willappreciate that other compounds may be used as the organosilanecomponent of the disclosed hybrid coating without departing from thescope of the present disclosure.

The metal alkoxide component may be the inorganic portion of thedisclosed hybrid coating. In one exemplary aspect, the metal alkoxidecomponent may be an aluminum alkoxide, such as aluminum s-butoxide,aluminum n-butoxide and aluminum t-butoxide. In a second exemplaryaspect, the metal alkoxide component may be a cerium alkoxide, such ascerium IV isopropoxide, cerium IV methoxyethoxide and cerium III2,4-pentanedionate. Those skilled in the art will appreciate that othermetal alkoxides may be used as the metal alkoxide component of thedisclosed hybrid coating without departing from the scope of the presentdisclosure.

Thus, the disclosed hybrid coating may be a hybrid material thatincludes both an organic component and an inorganic component.

Without being limited to any particular theory, the surfactant componentof the disclosed hybrid coating may improve the wet adhesion of thecoating by reducing the surface tension of the coating. In one exemplaryaspect, the surfactant component may be a liquid, nonionic surfactant,such as a straight chain primary aliphatic alkoxylated alcohol. Aspecific example of such a surfactant is ANTAROX® BL-240(CAS#68603-25-8), available from Rhodia Operations of Aubervilliers,France. However, those skilled in the art will appreciate that othersurfactants may be used as the surfactant component of the disclosedhybrid coating without departing from the scope of the presentdisclosure.

The relative quantities of the organosilane, metal alkoxide andsurfactant components may be selected to optimize the abrasionresistance, clarity, surface wetting, curability or other physicalproperties of the disclosed hybrid coating. In one exemplary aspect, themetal alkoxide and organosilane components may be present in thedisclosed coating at a molar ratio of about 2:1 (2 moles of the metalalkoxide component to 1 mole of the organosilane component) and thesurfactant component may be present at a molar ratio of 75:1 withrespect to the metal alkoxide component (75 moles of the metal alkoxidecomponent to 1 mole of the surfactant component). However, those skilledin the art will appreciate that the quantities (or molar ratios) mayvary depending on the constituents, the physical properties beingoptimized, or the specific needs of the user.

In one aspect, the disclosed hybrid coating may be prepared by combiningappropriate quantities of the organosilane, metal alkoxide andsurfactant components, optionally with a sufficient quantity of water,in a mixing vessel. The composition may be heated while continuouslystirring until the solution becomes clear. The clear solution may becooled to room temperature (e.g., about 25° C.) and then filtered. Inone particular aspect, the filtering step may be performed to removeparticles greater than about 10 μm. For example, Whatman #1 qualitativefilter paper, which has a manufacturer stated particle retention ratingof 11 μm, may be used.

At this point, those skilled in the art will appreciate that theresulting clear, cooled and filtered liquid may be a sol gel.

EXAMPLE 1 Hybrid Coating

A hybrid coating is prepared by combining 11.7 milliliters of 75 percentaluminum s-butoxide in s-butanol, 15.1 milliliters of(3-glycidoxypropyl)trimethoxysilane, 0.5 milliliters of 10 weightpercent ANTAROX® BL-240, and 22.7 milliliters of deionized water in aheat resistant vessel. The mixture is heated to a temperature of 90° C.while stirring. Stirring continues for an additional 120 minutes oruntil the mixture is clear. The mixture is then removed from the heatsource and allowed to cool to 25° C. The cooled mixture is then passedthrough Whatman #1 qualitative filter paper and the filtrand isdiscarded. The filtrate is stored in an air-tight container.

As discussed below, the disclosed hybrid coating may be used to coatvarious substrates, such as acrylic (e.g., stretched acrylic) and glass,as an initial coating or as a replenishment coating. Those skilled inthe art will appreciate that substrates other than acrylic and glass maybe coated with the disclosed hybrid coating without departing from thescope of the present disclosure.

Referring to FIG. 1, one method for applying a hybrid coating, generallydesignated 10, may begin by preparing the disclosed hybrid coating, asshown in block 12. The preparation of the disclosed hybrid coating hasbeen described in detail above.

As shown in block 14, an adhesion promoter may be prepared. The adhesionpromoter may be any material that may promote the adhesion of thedisclosed hybrid coating to the underlying substrate. One exemplaryadhesion promoter includes 2.5 percent by weight3-aminopropyltriethoxysilane in water. However, those skilled in the artwill appreciate that various adhesion promoting compositions may beused.

As shown in block 16, the surface of the substrate that will receive thecoating may be properly cleaned. Various techniques for cleaningsurfaces that will receive coatings are well known in the art. Forexample, when the substrate is stretched acrylic, the surface of thesubstrate may be wiped with isopropyl alcohol.

Furthermore, as shown in block 18, the cleaned surface of the substratemay be treated with oxygen plasma, though other treatments such ascorona may be used without departing from the scope of the presentdisclosure. The oxygen plasma may be generated with an open air plasmatreat system and may have a head that travels about 0.1 inches persecond at a distance of about 0.75 inches from the surface of thesubstrate. As an example, the oxygen plasma may be generated using theSPI Plasma-Prep™ plasma etcher available from Structure Probe, Inc. ofWest Chester, Pa. Without being limited to any particular theory, it isbelieved that the oxygen plasma and the surfactant in the disclosedhybrid coating both contribute to improving the wettability and theadhesion of the hybrid coating to the substrate.

After the cleaning (block 16) and plasma treating (block 18) steps, theadhesion promoter may be applied to the surface of the substrate, asshown in block 20. While various techniques may be used to apply theadhesion promoter, one exemplary technique is spraying. Then, as shownin block 22, the adhesion promoter may be allowed to cure if necessary.For example, when a 2.5 percent by weight solution of3-aminopropyltriethoxysilane in water is used as the adhesion promoter,the adhesion promoter may be cured for 10 minutes at 80° C., after whichthe substrate may be allowed to cool (block 24).

At this point, those skilled in the art will appreciate that the stepsshown in blocks 14 through 24 may be omitted as desired. In particular,the use of an adhesion promoter (i.e., the steps shown in blocks 14, 20,22 and 24) may be optionally omitted when the disclosed hybrid coatingis used as a replenishing coating. Also, the oxygen plasma treatment(block 18) may be optionally omitted when the disclosed hybrid coatingis used as a replenishing coating.

As shown in block 26, the hybrid coating may be applied to the surfaceof the cleaned and treated substrate. While spraying the hybrid coatingonto the substrate is one appropriate application technique, thoseskilled in the art will appreciate that various application techniques,such as drawing, blade coating and painting, may be used withoutdeparting from the scope of the present disclosure.

As shown in block 28, the hybrid coating applied to the substrate may becured before entering service. While the curing technique, including thecuring time and curing temperature, may vary depending on the specificcomposition of the hybrid coating, if the hybrid coating described inExample 1 above is used, a suitable cure should be obtained by restingat room temperature for about 16 hours followed by curing at 80° C. forabout 2 hours. After curing, the coated substrate may be allowed tocool, as shown in block 30.

Hybrid coatings (“Hybrid”) were tested on stretched acrylic for wet anddry adhesion in accordance with BSS7225, Class 5 (adhesion of 7 is theminimum requirement and 10 is perfect adhesion). Aluminum s-butoxide wasused as the metal alkoxide component (“Inorganic”),(3-glycidoxypropyl)trimethoxysilane was used as the organosilanecomponent (“Organic”) and ANTAROX® BL-240 was used as the surfactantcomponent. Oxygen plasma (“Plasma”), corona treatment (“Corona”) and anadhesion promoter (“AP”) were used where indicated. The results areshown in Table 1.

TABLE 1 Organic to Plasma Plasma Inorganic Speed Height Dry Wet Stack UpRatio (in/s) (in) Adhesion Adhesion Hybrid (only) 2 0 0 1 1 Coronoa +AP + 2 (60 s) 2 10 3 Hybrid Plasma + AP + 2 0.5 0.4 8 5 Hybrid Plasma +AP + 2 0.25 0.7 9 8 Hybrid Plasma + AP + 2 0.1 0.7 10 10 Hybrid Plasma +AP + 2 0.05 0.7 10 10 Hybrid Plasma + AP + 4 0.1 0.7 2 1 Hybrid

Thus, the disclosed hybrid coatings yield good dry and wet adhesion,particularly when applied using the disclosed methods.

Filtered and unfiltered hybrid coatings having aluminum s-butoxide toANTAROX® BL-240 ratios of 150:1 and 75:1 were tested on stretchedacrylic for haze and clarity. The results are shown in Table 2.

TABLE 2 Inorganic to Surfactant Sample Filtered Ratio Haze StandardClarity Standard 1 No 150:1  2.05 <1.0 98.2 >99.0 2 Yes 1.51 1.51 <1.098.5 >99.0 3 No 75:1 1.25 <1.0 99.6 >99.0 4 Yes 75:1 0.22 <1.0 99.8>99.0

Thus, the disclosed hybrid coatings yield low initial haze and highinitial clarity.

The abrasion resistance of the disclosed hybrid coatings on stretchedacrylic was assessed using ASTM D 1044, which is commonly referred to asthe Taber abrasion test. The results are shown in FIGS. 2-7.

FIG. 2 shows percent haze obtained after 100 cycles of abrasion on bareacrylic, acrylic treated with a polysiloxane only (prior art), andacrylic treated with the disclosed hybrid coating. FIG. 3 shows percenthaze versus abrasion cycles for a bare acrylic substrate and an acrylicsubstrate coated with the disclosed hybrid coating. FIG. 4 shows percenthaze versus abrasion cycles for a worn acrylic substrate replenishedwith the disclosed hybrid coating. FIG. 5 shows percent haze versusabrasion cycles for an acrylic substrate coated with the disclosedhybrid coating, subjected to approximately 1600 abrasion cycles,replenished with the disclosed hybrid coating, then again subjected toabrasion. FIG. 6 shows percent haze versus abrasion cycles for anacrylic substrate coated with a prior art coating, subjected toapproximately 100 abrasion cycles, replenished with the disclosed hybridcoating, then again subjected to abrasion. FIG. 7 shows percent hazeversus abrasion cycles for an acrylic substrate initially coated with aduplex coating (i.e., a first layer of prior art coating with a top coatof the disclosed hybrid coating), subjected to approximately 2500abrasion cycles, replenished with the disclosed hybrid coating, thenagain subjected to abrasion.

Thus, the disclosed hybrid coatings provide substantially improvedabrasion resistance, whether used as an initial coating or as areplenishing coating.

Accordingly, the disclosed hybrid coatings yield low initial haze andhigh initial clarity, good dry and wet adhesion (particularly tostretched acrylic), and excellent abrasion resistance. Furthermore, thedisclosed hybrid coatings may be used as replenishment coatings torestore the clarity and abrasion resistance to worn substrates,regardless of whether the substrates have been previously coated. Stillfurthermore, the disclosed hybrid coatings may be prepared as an aqueoussol-gel material and, therefore, are environmentally friendly.

Although various aspects of the disclosed hybrid coatings and associatedmethods of application have been shown and described, modifications mayoccur to those skilled in the art upon reading the specification. Thepresent application includes such modifications and is limited only bythe scope of the claims.

What is claimed:
 1. A hybrid coating composition comprising: anorganosilane component, a metal alkoxide component, and a surfactantcomponent, wherein the metal alkoxide component is present in thecomposition at a molar ratio of about 75:1 with respect to thesurfactant component; and wherein the hybrid coating composition oncecured on a transparent substrate has an initial clarity greater than 98.2. The hybrid coating composition of claim 1, wherein the hybrid coatingcomposition further comprises water.
 3. The hybrid coating compositionof claim 1, wherein the hybrid coating composition is a sol gel.
 4. Thehybrid coating composition of claim 1, wherein the hybrid coatingcomposition is substantially free of particles greater than 11 μm. 5.The hybrid coating composition of claim 1, wherein the organosilanecomprises one or more of (3-glycidoxypropyl)trimethoxysilane,3-glycidoxypropyltriethoxysilane, paminophenylsilane,allyltrimethoxysilane, n-(2-aminoethyl)-3-aminopropyltrimethoxysilane,3-aminopropyltriethoxysilane, 3-aminopropyltrimethoxysilane,3-glycidoxypropyldiisopropylethoxysilane,(3-glycidoxypropyl)methyldiethoxysilane,3-mercaptopropyltrimethoxysilane, 3-mercaptopropyltriethoxysilane,3-methacryloxypropylmethyldiethoxysilane,3-methacryloxypropylmethyldimethoxysilane,3methacryloxypropyltrimethoxysilane,n-phenylaminopropyltrimethoxysilane, vinylmethyldiethoxysilane,vinyltriethoxysilane, vinyltrimethoxysilane, tetraethylorthosilicate. 6.The hybrid coating composition of claim 5, wherein the metal alkoxidecomprises one or more of aluminum s-butoxide, aluminum n-butoxide, andaluminum t-butoxide.
 7. The hybrid coating composition of claim 5,wherein the metal alkoxide comprises one or more of cerium IVisopropoxide, cerium IV methoxyethoxide, and cerium III2,4-pentanedionate.
 8. The hybrid coating composition of claim 1,wherein the surfactant component comprises a straight chain primaryaliphatic alkoxylated alcohol.
 9. A transparent member comprising: atransparent substrate having a hybrid coating composition cured on afirst major surface thereof, the hybrid coating composition comprising:an organosilane component, a metal alkoxide component, and a surfactantcomponent, wherein the metal alkoxide component is present in thecomposition at a molar ratio of about 75:1 with respect to thesurfactant component; and wherein the hybrid coating has a claritygreater than
 98. 10. The transparent member of claim 9, wherein thefirst major surface of the transparent substrate is an oxygen plasmatreated surface or a corona treated surface with the hybrid coatingcomposition cured thereto.
 11. The transparent member of claim 9,further comprising an adhesion promoter between the transparentsubstrate and the hybrid coating composition.
 12. The transparent memberof claim 11, wherein the adhesion promoter comprises a solution of3-aminopropyltriethoxysilane in water.
 13. The transparent member ofclaim 9, wherein the hybrid coating composition is substantially free ofparticles greater than 11 μm.
 14. The transparent member of claim 9,wherein the organosilane comprises one or more of(3-glycidoxypropyl)trimethoxysilane, 3-glycidoxypropyltriethoxysilane,paminophenylsilane, allyltrimethoxysilane,n-(2-aminoethyl)-3-aminopropyltrimethoxysilane,3-aminopropyltriethoxysilane, 3-aminopropyltrimethoxysilane,3-glycidoxypropyldiisopropylethoxysilane,(3-glycidoxypropyl)methyldiethoxysilane,3-mercaptopropyltrimethoxysilane, 3-mercaptopropyltriethoxysilane,3-methacryloxypropylmethyldiethoxysilane,3-methacryloxypropylmethyldimethoxysilane,3methacryloxypropyltrimethoxysilane,n-phenylaminopropyltrimethoxysilane, vinylmethyldiethoxysilane,vinyltriethoxysilane, vinyltrimethoxysilane, tetraethylorthosilicate.15. The transparent member of claim 14, wherein the metal alkoxidecomprises one or more of aluminum s-butoxide, aluminum n-butoxide, andaluminum t-butoxide.
 16. The transparent member of claim 14, wherein themetal alkoxide comprises one or more of cerium IV isopropoxide, ceriumIV methoxyethoxide, and cerium III 2,4-pentanedionate.
 17. Thetransparent member of claim 9, wherein the surfactant componentcomprises a straight chain primary aliphatic alkoxylated alcohol. 18.The transparent member of claim 9, wherein the metal alkoxide componentis present in the composition at a molar ratio of about 2:1 with respectto the organosilane component.
 19. The transparent member of claim 9,wherein the transparent substrate is a window or windshield comprisingstretched acrylic or glass.
 20. The transparent member of claim 9,wherein the hybrid coating composition further comprises water.